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rs1939875

From SNPedia

Orientationminus
Stabilizedminus
Make rs1939875(C;C)
Make rs1939875(C;T)
Make rs1939875(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position95689703
is asnp
is mentioned by
dbSNPrs1939875
ebirs1939875
HLIrs1939875
Exacrs1939875
Varsomers1939875
Maprs1939875
PheGenIrs1939875
hapmaprs1939875
1000 genomesrs1939875
hgdprs1939875
ensemblrs1939875
gopubmedrs1939875
geneviewrs1939875
scholarrs1939875
googlers1939875
pharmgkbrs1939875
gwascentralrs1939875
openSNPrs1939875
23andMers1939875
23andMe allrs1939875
SNP Nexus

SNPshotrs1939875
SNPdbers1939875
MSV3drs1939875
GWAS Ctlgrs1939875
GMAF0.253
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20208534OA-icon.png]
Trait Eosinophilic esophagitis (pediatric)
Title Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Risk Allele T
P-val 0.000003
Odds Ratio 1.54 [1.22-1.93]